INMODE WMBODY DEVICE— 510(k) K131362

Substantially Equivalent

Inmode MD , Ltd.

FDA 510(k) clearance K131362 for INMODE WMBODY DEVICE, Substantially Equivalent on 2013-10-08. Applicant: Inmode MD , Ltd.. Device class: 2.

Clearance details

Applicant: Inmode MD , Ltd.
Product code: Code NUV
Device class: Class 2
Regulation: 21 CFR 878.4810
Advisory panel: General, Plastic Surgery
Date received: 2013-05-13
Decision date: 2013-10-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kfar Saba, IL

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.